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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1992-2-21
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pubmed:abstractText |
Reference strains of Escherichia coli (ampicillin-susceptible and -resistant ATCC strains, and known TEM-1 and TEM-2 beta-lactamase producers) were tested in vitro and in the in-vivo mouse thigh infection model against four beta-lactamase inhibitor compounds (BICs: amoxycillin/clavulanic acid, ampicillin/sulbactam, ticarcillin/clavulanic acid, and piperacillin/tazobactam), selected cephalosporins, and imipenem. The ATCC strains (ampicillin-susceptible and -resistant) were susceptible to the BICs in disc and MIC tests. Three or more logs of killing were observed at the NCCLS breakpoint concentrations. However, the TEM-1 and TEM-2 producers were resistant in disc tests to ampicillin/sulbactam and amoxycillin/clavulanic acid, and showed intermediate susceptibility to ticarcillin/clavulanic acid. MICs were at or near the breakpoint, but bactericidal activity was only noted at the probable breakpoint concentration of piperacillin/tazobactam. Cefoxitin, cefotaxime, cefpirome and imipenem, but not cephalothin, showed greater bactericidal activity and lower MICs for the TEM-producing strains than the BICs. The viable count of the TEM-1 producer was not reduced in the mouse thigh model by ampicillin/sulbactam or amoxycillin/clavulanic acid, but cefpirome and cefotaxime reduced the viable count by approximately three logs. There was a 50% mortality rate in mice receiving the two BICs. The ampicillin-susceptible ATCC strain of E. coli was killed to a similar degree by all agents tested. Overall, the BICs appeared inferior, in both in-vivo and in-vitro tests to selected cephalosporins and imipenem when tested against reference strains of E. coli producing TEM-1 or TEM-2 beta-lactamase. The large inoculum effect and poor bactericidal activity observed with the BICs suggest they could be less effective in certain clinical situations.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Bacterial Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Cephalosporins,
http://linkedlifedata.com/resource/pubmed/chemical/Imipenem,
http://linkedlifedata.com/resource/pubmed/chemical/beta-Lactamases,
http://linkedlifedata.com/resource/pubmed/chemical/beta-lactamase TEM-1,
http://linkedlifedata.com/resource/pubmed/chemical/beta-lactamase TEM-2
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0305-7453
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
61-70
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pubmed:dateRevised |
2008-9-4
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pubmed:meshHeading |
pubmed-meshheading:1769944-Animals,
pubmed-meshheading:1769944-Anti-Bacterial Agents,
pubmed-meshheading:1769944-Cell Cycle,
pubmed-meshheading:1769944-Cephalosporins,
pubmed-meshheading:1769944-Colony Count, Microbial,
pubmed-meshheading:1769944-Diffusion,
pubmed-meshheading:1769944-Drug Therapy, Combination,
pubmed-meshheading:1769944-Escherichia coli,
pubmed-meshheading:1769944-Female,
pubmed-meshheading:1769944-Imipenem,
pubmed-meshheading:1769944-Mice,
pubmed-meshheading:1769944-Microbial Sensitivity Tests,
pubmed-meshheading:1769944-beta-Lactamases
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pubmed:year |
1991
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pubmed:articleTitle |
An in-vitro and in-vivo comparison of the activity of beta-lactamase inhibitor combinations with imipenem and cephalosporins against Escherichia coli producing TEM-1 or TEM-2 beta-lactamase.
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pubmed:affiliation |
Department of Medicine, Mercy Hospital of Medical Center, Chicago, Illinois 60616-2477.
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pubmed:publicationType |
Journal Article,
Comparative Study
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